A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3308132



Internal ID15155080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87894599..87894600hg38UCSC Ensembl
Innerchr9:87894566..87894633hg38UCSC Ensembl
Outerchr9:87894565..87894634hg38UCSC Ensembl
chr9:90509514..90509515hg19UCSC Ensembl
Innerchr9:90509481..90509548hg19UCSC Ensembl
Outerchr9:90509480..90509549hg19UCSC Ensembl
chr9:89699334..89699335hg18UCSC Ensembl
Innerchr9:89699368..89699301hg18UCSC Ensembl
Outerchr9:89699300..89699369hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3880
hg1980
hg1880
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7838884
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3308132
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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